Ingenia Elition S — Class II medical device recall Z-0694-2019
Terminated recall by Philips Medical Systems Nederlands, reported 2019-01-16, distributed in CA, MN, NJ, NY, OH, TN, TX. During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected resta
| Recall number | Z-0694-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems Nederlands, Best, Netherlands |
| Recall initiated | 2018-12-03 |
| Classified | 2019-01-08 |
| Reported by FDA | 2019-01-16 |
| Terminated | 2020-05-12 |
| Distributed | CA, MN, NJ, NY, OH, TN, TX |
| Countries outside the US | AE, BE, CA, CH, DE, FR, IN, NL, SE, ZA |
| Quantity | 35 |
| Serial numbers | 45007, 45008, 45010, 45011, 45024, 45025, 45026, 45027, 45028, 45029, 45030, 45031, 45032, 45033, 45034, 45035, 45037, 45039, 45040, 45042, 45043, 45044, 45045, 45046, 45048 and 10 more |
Product
Ingenia Elition S, Ingenia Elition X
Reason for recall
During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0694-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.